Expressions of protein oxidation markers, dityrosine and advanced oxidation protein products in Cisplatin-induced nephrotoxicity in rats

J Vet Med Sci. 2011 Mar;73(3):403-7. doi: 10.1292/jvms.10-0371. Epub 2010 Nov 1.

Abstract

The purpose of this study was to evaluate whether dityrosine and advanced oxidation protein products (AOPP) reflect the severity of cisplatin-induced nephrotoxicity. Immunoexpression of dityrosine in kidneys and plasma AOPP concentration were examined up to day 4 post-cisplatin injection in rats. Cisplatin injection induced tubular injury on days 2-4 after injection and increased serum creatinine and BUN on days 3 and 4. On days 2-4, dityrosine was immunostained in the cytoplasm of damaged tubular cells, and their immunostaining intensity increased time-dependently. Plasma AOPP levels were significantly increased on days 3 and 4. These results suggest that expressions of dityrosine and AOPP were associated with the severity of renal injury and may be useful markers for the development of cisplatin-induced nephrotoxicity.

MeSH terms

  • Animals
  • Antineoplastic Agents / toxicity*
  • Biomarkers / blood
  • Biomarkers / metabolism
  • Cisplatin / toxicity*
  • Gene Expression Regulation / physiology*
  • Kidney Diseases / chemically induced*
  • Kidney Diseases / metabolism
  • Oxidation-Reduction
  • Rats
  • Time Factors
  • Tyrosine / analogs & derivatives*
  • Tyrosine / blood
  • Tyrosine / metabolism

Substances

  • Antineoplastic Agents
  • Biomarkers
  • Tyrosine
  • dityrosine
  • Cisplatin